MedPath

Nitrofurantoin Monohydrate/ Macrocrystalline

Nitrofurantoin Monohydrate/Macrocrystals Capsules

Approved
Approval ID

a310b8cd-3390-4648-943c-328d409ca8e3

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 26, 2018

Manufacturers
FDA

Central Texas Community Health Centers

DUNS: 079674019

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Nitrofurantoin Monohydrate/Macrocrystalline

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code76413-165
Application NumberNDA020064
Product Classification
M
Marketing Category
C73594
G
Generic Name
Nitrofurantoin Monohydrate/Macrocrystalline
Product Specifications
Route of AdministrationORAL
Effective DateJune 20, 2012
FDA Product Classification

INGREDIENTS (14)

NITROFURANTOINActive
Quantity: 25 mg in 1 1
Code: 927AH8112L
Classification: ACTIB
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)Inactive
Code: Z135WT9208
Classification: IACT
FD&C RED NO. 40Inactive
Code: WZB9127XOA
Classification: IACT
GELATIN, UNSPECIFIEDInactive
Code: 2G86QN327L
Classification: IACT
POVIDONE, UNSPECIFIEDInactive
Code: FZ989GH94E
Classification: IACT
LACTOSE, UNSPECIFIED FORMInactive
Code: J2B2A4N98G
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
SUCROSEInactive
Code: C151H8M554
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
NITROFURANTOIN MONOHYDRATEActive
Quantity: 75 mg in 1 1
Code: E1QI2CQQ1I
Classification: ACTIM

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